A genome wide dosage suppressor network reveals genomic robustness

Autor: Jesse P. Frumkin, Arend Hintze, Eric M. Phizicky, Bruz Marzolf, Alpan Raval, Biranchi N. Patra, Nitin S. Baliga, Amardeep Kaur, Elizabeth J. Grayhack, Ashish Bhan, Jenna K. Tamashiro, David J. Galas, Anthony W. Sevold, Christoph Adami, Ravishankar R. Vallabhajosyula, Gitanjali Yadav, Bjørn Østman, Jory Schossau, Yoshiko Kon, Animesh Ray
Přispěvatelé: Ray, Animesh [0000-0002-0120-5820], Apollo - University of Cambridge Repository
Jazyk: angličtina
Rok vydání: 2016
Předmět:
cell division
0301 basic medicine
Gene regulatory network
Gene Dosage
gene regulatory network
genetic analysis
Lethal
Genome
0302 clinical medicine
Gene Expression Regulation
Fungal

genetic parameters
genome wide dosage suppressor
genetics
Gene Regulatory Networks
Genetics
Regulation of gene expression
biology
correlational study
Biochemistry and Molecular Biology
reproductive fitness
gene expression regulation
Genomics
3. Good health
Fungal
RNA polymerase
fungal genome
RNA polymerase II
RNA Polymerase II
Genome
Fungal

cell cycle regulation
Cell Division
Saccharomyces cerevisiae Proteins
Saccharomyces cerevisiae
gene repression
gene dosage
DNA replication
Biology
Gene dosage
Article
03 medical and health sciences
Saccharomyces cerevisiae protein
lethal gene
gene expression profiling
mutant
protein interaction
RNA synthesis
Gene
gene interaction
Gene Expression Profiling
Robustness (evolution)
Computational Biology
bacterial strain
biology.organism_classification
Gene expression profiling
gene function
030104 developmental biology
RNA processing
Genes
protein analysis
Mutation
gene expression
Genes
Lethal

microarray analysis
Genetic Fitness
mutation
metabolism
genomic robustness
Biokemi och molekylärbiologi
030217 neurology & neurosurgery
Zdroj: Nucleic Acids Research
ISSN: 1362-4962
0305-1048
Popis: Genomic robustness is the extent to which an organism has evolved to withstand the effects of deleterious mutations. We explored the extent of genomic robustness in budding yeast by genome wide dosage suppressor analysis of 53 conditional lethal mutations in cell division cycle and RNA synthesis related genes, revealing 660 suppressor interactions of which 642 are novel. This collection has several distinctive features, including high cooccurrence of mutant-suppressor pairs within protein modules, highly correlated functions between the pairs and higher diversity of functions among the co-suppressors than previously observed. Dosage suppression of essential genes encoding RNA polymerase subunits and chromosome cohesion complex suggests a surprising degree of functional plasticity of macromolecular complexes, and the existence of numerous degenerate pathways for circumventing the effects of potentially lethal mutations. These results imply that organisms and cancer are likely able to exploit the genomic robustness properties, due the persistence of cryptic gene and pathway functions, to generate variation and adapt to selective pressures. © 2016 The Author(s).
Databáze: OpenAIRE